ClinVar Miner

List of variants in gene ABCC9 reported by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 145
Download table as spreadsheet
HGVS dbSNP
NM_005691.3(ABCC9):c.1011+7T>C rs1224367944
NM_005691.3(ABCC9):c.1012-1G>C rs878854781
NM_005691.3(ABCC9):c.1022C>T (p.Thr341Ile) rs1565475592
NM_005691.3(ABCC9):c.1056C>T (p.Tyr352=) rs149408382
NM_005691.3(ABCC9):c.1127C>T (p.Thr376Ile) rs372244832
NM_005691.3(ABCC9):c.1165-2A>G rs878854782
NM_005691.3(ABCC9):c.1165-5G>T rs1411076886
NM_005691.3(ABCC9):c.1212C>T (p.Ser404=) rs376726505
NM_005691.3(ABCC9):c.1262C>T (p.Thr421Ile)
NM_005691.3(ABCC9):c.1296C>T (p.Pro432=) rs10770865
NM_005691.3(ABCC9):c.1332C>T (p.Gly444=) rs369830406
NM_005691.3(ABCC9):c.133T>C (p.Leu45=) rs1555125400
NM_005691.3(ABCC9):c.136T>C (p.Phe46Leu) rs1555125391
NM_005691.3(ABCC9):c.1374C>T (p.Val458=) rs200819464
NM_005691.3(ABCC9):c.1375G>A (p.Gly459Ser) rs1060503051
NM_005691.3(ABCC9):c.1381G>C (p.Ala461Pro) rs374535641
NM_005691.3(ABCC9):c.1416T>C (p.Phe472=) rs777308898
NM_005691.3(ABCC9):c.1524T>C (p.Tyr508=) rs1555112390
NM_005691.3(ABCC9):c.1557G>A (p.Glu519=) rs143346402
NM_005691.3(ABCC9):c.1577T>G (p.Leu526Arg) rs1555112333
NM_005691.3(ABCC9):c.1603T>C (p.Tyr535His) rs397517184
NM_005691.3(ABCC9):c.1618+6T>C
NM_005691.3(ABCC9):c.1619-7T>C rs769816456
NM_005691.3(ABCC9):c.1677G>A (p.Ala559=) rs76458291
NM_005691.3(ABCC9):c.1785A>G (p.Ala595=) rs1555106091
NM_005691.3(ABCC9):c.1817A>C (p.Asn606Thr) rs149229372
NM_005691.3(ABCC9):c.1848C>T (p.Asp616=) rs61001398
NM_005691.3(ABCC9):c.1849G>A (p.Asp617Asn) rs757681761
NM_005691.3(ABCC9):c.1874C>T (p.Ser625Leu)
NM_005691.3(ABCC9):c.1879C>G (p.Pro627Ala) rs367770980
NM_005691.3(ABCC9):c.1887G>T (p.Glu629Asp) rs150036969
NM_005691.3(ABCC9):c.1899_1901dup (p.His634_Thr635insGln)
NM_005691.3(ABCC9):c.1933A>G (p.Lys645Glu) rs876657734
NM_005691.3(ABCC9):c.1942G>C (p.Gly648Arg) rs368279608
NM_005691.3(ABCC9):c.1975A>G (p.Thr659Ala) rs878854783
NM_005691.3(ABCC9):c.1979G>A (p.Arg660Gln) rs150255709
NM_005691.3(ABCC9):c.1993G>A (p.Ala665Thr) rs200891785
NM_005691.3(ABCC9):c.2011G>A (p.Ala671Thr) rs1220942080
NM_005691.3(ABCC9):c.2045G>A (p.Gly682Asp) rs752106985
NM_005691.3(ABCC9):c.2050G>A (p.Gly684Ser) rs148174226
NM_005691.3(ABCC9):c.2072T>C (p.Ile691Thr) rs766197122
NM_005691.3(ABCC9):c.2093-7T>C rs185235724
NM_005691.3(ABCC9):c.2154C>T (p.Ile718=) rs74067815
NM_005691.3(ABCC9):c.2157C>T (p.Leu719=) rs201848437
NM_005691.3(ABCC9):c.215G>A (p.Arg72Lys) rs369409311
NM_005691.3(ABCC9):c.2198+1G>A
NM_005691.3(ABCC9):c.2198+3A>G rs1555194960
NM_005691.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2222T>C (p.Phe741Ser)
NM_005691.3(ABCC9):c.2238-1G>A rs141281214
NM_005691.3(ABCC9):c.2262T>C (p.Tyr754=) rs145561881
NM_005691.3(ABCC9):c.23A>G (p.Asn8Ser)
NM_005691.3(ABCC9):c.2408C>T (p.Thr803Ile) rs997660720
NM_005691.3(ABCC9):c.2424+3G>A
NM_005691.3(ABCC9):c.2424+9T>C rs11835804
NM_005691.3(ABCC9):c.2495T>C (p.Ile832Thr)
NM_005691.3(ABCC9):c.2500T>C (p.Phe834Leu) rs367776754
NM_005691.3(ABCC9):c.2522C>T (p.Ala841Val) rs1555189354
NM_005691.3(ABCC9):c.2523C>T (p.Ala841=) rs144537241
NM_005691.3(ABCC9):c.2554C>T (p.Gln852Ter) rs193922683
NM_005691.3(ABCC9):c.2574C>T (p.Phe858=) rs1273498300
NM_005691.3(ABCC9):c.2591G>A (p.Arg864Lys)
NM_005691.3(ABCC9):c.2599G>A (p.Val867Ile) rs376754153
NM_005691.3(ABCC9):c.2630C>T (p.Thr877Met) rs140872303
NM_005691.3(ABCC9):c.2631G>A (p.Thr877=) rs139408145
NM_005691.3(ABCC9):c.2643+6A>G rs1565740203
NM_005691.3(ABCC9):c.2784C>G (p.Asp928Glu) rs139472403
NM_005691.3(ABCC9):c.2826T>C (p.Tyr942=) rs141025897
NM_005691.3(ABCC9):c.2856C>T (p.Asp952=) rs758697683
NM_005691.3(ABCC9):c.2857G>A (p.Glu953Lys) rs143685061
NM_005691.3(ABCC9):c.2862C>T (p.Asp954=) rs2291550
NM_005691.3(ABCC9):c.2865A>T (p.Glu955Asp) rs922212635
NM_005691.3(ABCC9):c.287G>A (p.Arg96Gln) rs202103893
NM_005691.3(ABCC9):c.2889_2891del (p.Glu963del) rs1555187363
NM_005691.3(ABCC9):c.293A>G (p.Glu98Gly)
NM_005691.3(ABCC9):c.2961A>G (p.Thr987=) rs1555187333
NM_005691.3(ABCC9):c.2965G>A (p.Gly989Arg)
NM_005691.3(ABCC9):c.3030T>C (p.Ala1010=) rs76102634
NM_005691.3(ABCC9):c.305T>C (p.Leu102Pro) rs374659816
NM_005691.3(ABCC9):c.3095A>G (p.Gln1032Arg) rs757471451
NM_005691.3(ABCC9):c.3245+3A>C
NM_005691.3(ABCC9):c.3267G>A (p.Leu1089=) rs780998911
NM_005691.3(ABCC9):c.3315+6T>C rs201117578
NM_005691.3(ABCC9):c.3316-4A>C rs201147809
NM_005691.3(ABCC9):c.3321C>T (p.Ile1107=) rs35404804
NM_005691.3(ABCC9):c.3331T>C (p.Leu1111=) rs764155671
NM_005691.3(ABCC9):c.3339T>G (p.Ser1113=) rs138280089
NM_005691.3(ABCC9):c.3346C>T (p.Arg1116Cys) rs387907228
NM_005691.3(ABCC9):c.3357G>A (p.Leu1119=) rs2287626
NM_005691.3(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473
NM_005691.3(ABCC9):c.3440A>G (p.Tyr1147Cys) rs1060503052
NM_005691.3(ABCC9):c.3460C>T (p.Arg1154Trp) rs387907208
NM_005691.3(ABCC9):c.3461G>A (p.Arg1154Gln) rs387907209
NM_005691.3(ABCC9):c.3574A>G (p.Thr1192Ala) rs1437273344
NM_005691.3(ABCC9):c.3589C>T (p.Arg1197Cys) rs778849288
NM_005691.3(ABCC9):c.3590G>A (p.Arg1197His) rs755156050
NM_005691.3(ABCC9):c.3594G>A (p.Met1198Ile) rs199900459
NM_005691.3(ABCC9):c.3621T>C (p.Ile1207=) rs767458242
NM_005691.3(ABCC9):c.3669+1G>C
NM_005691.3(ABCC9):c.3669G>A (p.Thr1223=) rs146942382
NM_005691.3(ABCC9):c.3729G>A (p.Ser1243=) rs140182559
NM_005691.3(ABCC9):c.372T>C (p.Asn124=) rs377384557
NM_005691.3(ABCC9):c.3768T>C (p.Leu1256=) rs150303433
NM_005691.3(ABCC9):c.3772-4A>C rs1555179333
NM_005691.3(ABCC9):c.377A>G (p.Glu126Gly) rs1060503054
NM_005691.3(ABCC9):c.3796G>A (p.Val1266Met) rs1555179320
NM_005691.3(ABCC9):c.3893-3C>T rs762931725
NM_005691.3(ABCC9):c.3982G>A (p.Val1328Ile) rs1060503053
NM_005691.3(ABCC9):c.3993C>T (p.His1331=) rs377704379
NM_005691.3(ABCC9):c.3994G>A (p.Val1332Ile) rs200350065
NM_005691.3(ABCC9):c.3999G>A (p.Lys1333=) rs1555178738
NM_005691.3(ABCC9):c.4014T>C (p.Pro1338=) rs1555178731
NM_005691.3(ABCC9):c.4062G>A (p.Ser1354=) rs145005748
NM_005691.3(ABCC9):c.4103-3C>T
NM_005691.3(ABCC9):c.4129A>G (p.Ile1377Val) rs1565687632
NM_005691.3(ABCC9):c.4202del (p.Gly1401fs)
NM_005691.3(ABCC9):c.4205C>G (p.Ser1402Cys)
NM_005691.3(ABCC9):c.4344T>C (p.Asn1448=) rs146782703
NM_005691.3(ABCC9):c.4353T>C (p.Val1451=) rs771226136
NM_005691.3(ABCC9):c.4437T>C (p.Ile1479=) rs368079660
NM_005691.3(ABCC9):c.4497C>T (p.Thr1499=) rs1060504811
NM_005691.3(ABCC9):c.4512+7A>G rs371646433
NM_005691.3(ABCC9):c.4512T>A (p.Ala1504=) rs777591544
NM_005691.3(ABCC9):c.4519G>A (p.Val1507Ile) rs876657737
NM_005691.3(ABCC9):c.457G>A (p.Val153Ile)
NM_005691.3(ABCC9):c.4591C>T (p.Pro1531Ser) rs142875103
NM_005691.3(ABCC9):c.4631T>C (p.Leu1544Ser)
NM_005691.3(ABCC9):c.47A>G (p.Asn16Ser) rs727502877
NM_005691.3(ABCC9):c.483C>G (p.Asp161Glu)
NM_005691.3(ABCC9):c.48C>T (p.Asn16=) rs199631710
NM_005691.3(ABCC9):c.497G>A (p.Arg166His)
NM_005691.3(ABCC9):c.4A>G (p.Ser2Gly) rs1485712335
NM_005691.3(ABCC9):c.5G>A (p.Ser2Asn) rs1359649036
NM_005691.3(ABCC9):c.789C>T (p.Cys263=) rs58386780
NM_005691.3(ABCC9):c.798T>C (p.Asp266=) rs138356189
NM_005691.3(ABCC9):c.816G>T (p.Lys272Asn)
NM_005691.3(ABCC9):c.817-14_817-4del rs774857795
NM_005691.3(ABCC9):c.837A>G (p.Pro279=) rs1264086698
NM_005691.3(ABCC9):c.884G>A (p.Arg295Gln)
NM_005691.3(ABCC9):c.918G>A (p.Leu306=) rs142115849
NM_005691.3(ABCC9):c.924T>C (p.Asp308=) rs139127928
NM_005691.3(ABCC9):c.959G>T (p.Gly320Val) rs200272254
NM_005691.3(ABCC9):c.970C>T (p.Arg324Cys) rs779720018
NM_020297.3(ABCC9):c.4512+744_4512+746delinsAAAT rs869025349
NM_020297.3(ABCC9):c.817-7del rs193922684

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.